![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[Supplementary Material]](/e/graphics/supplementarymaterialsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Open access]](/e/graphics/free.gif)
![[Contents scheme]](im2166contents.gif)
Acta Cryst. (2010). E66, o149 [ doi:10.1107/S1600536809053215 ]
Abstract: In the title compound, C19H14N4, which was crystallized from dimethyl sulfoxide, the arene and heterocyclic rings of the lophine analogue framework differ only slightly from coplanarity (dihedral angles range from 8.8 to 20.2°), and intramolecular N-H
N and C-H
N interactions help to establish the conformation. The crystal packing features a number of weak C-H
N, N-H
N hydrogen-bond type contacts, and C-H
interactions, leading to the formation of a herringbone structure.
Online 16 December 2009
Copyright © International Union of Crystallography
IUCr Webmaster